Simple, rapid nonradioactive method to detect the three most prevalent hereditary fructose intolerance mutations
Costa, C.; Costa, J.M.; Deleuze, J.F.; Legrand, A.; Hadchouel, M.; Baussan, C.
Clinical Chemistry 44(5): 1041-1043
1998
ISSN/ISBN: 0009-9147 PMID: 9590379 Document Number: 492477
Document emailed within 1 workday
Related Documents
Strasberg, P.M.; Clarke, J.T. 1992: Rapid nonradioactive tracer method for detecting carriers of the major Ashkenazi Jewish Tay-Sachs disease mutations Clinical Chemistry 38(11): 2249-2255Hackl, J.M.; Balogh, D.; Kunz, F.; Dworzak, E.; Puschendorf, B.; Decristoforo, A.; Maier, F. 1978: Postoperative fructose infusion in a case of presumed hereditary fructose intolerance Wiener Klinische Wochenschrift 90(7): 237-240
Nüssli, R. 1971: Growth of patients with hereditary fructose intolerance or hereditary saccharose-isomaltose malabsorption Helvetica Paediatrica Acta 26(5): 637-647
Lopez-Crapez, E.; Chypre, C.; Saavedra, J.; Marchand, J.; Grenier, J. 1997: Rapid and large-scale method to detect K-ras gene mutations in tumor samples Clinical Chemistry 43(6 Pt 1): 936-942
Varesco, L.; Groden, J.; Spirio, L.; Robertson, M.; Weiss, R.; Gismondi, V.; Ferrara, G.B.; White, R. 1993: A rapid screening method to detect nonsense and frameshift mutations: identification of disease-causing APC alleles Cancer Research 53(23): 5581-5584
Steinmann, B.; Gitzelmann, R. 1981: The diagnosis of hereditary fructose intolerance Helvetica Paediatrica Acta 36(4): 297-316
Mattes, S.; Schmidt, G. 1979: Hereditary fructose intolerance and therapeutic problems Kinderarztliche Praxis 47(1): 26-30
Mercier, J.C.; Bourrillon, A.; Beaufils, F.; Odievre, M. 1976: Hereditary fructose intolerance with early onset Archives Francaises de Pediatrie 33(10): 945-953
Coşkun, T.; Ozalp, I.; Tekinalp, G. 1991: Hereditary fructose intolerance in a patient with phenylketonuria Turkish Journal of Pediatrics 33(3): 181-184
Brauman, J.; Kentos, P.; Frisque, P.; Gepts, W.; Verbanck, M. 1971: Hereditary fructose intolerance in an 83-year-old woman Acta Clinica Belgica 26(2): 65-77
Dreyfus, J.C.; Schapira, F.; Besmond, C.; Gregori, C.; Kahn, A. 1985: Study of hereditary fructose intolerance by methods of molecular biology Annales de Medecine Interne 136(6): 456-458
Celiker, V.; Dural, O.; Erdem, K. 1993: Anesthetic management of a patient with hereditary fructose intolerance and phenylketonuria Turkish Journal of Pediatrics 35(2): 127-130
Di Martino, L.; Iorio, G.; Guandalini, S.; Iannuzzi, S.; Battaglia, A.; Andria, G. 1980: Hereditary fructose intolerance: description of 2 cases with early onset La Pediatria 88(1): 99-110
Okayama, H.; Curiel, D.T.; Brantly, M.L.; Holmes, M.D.; Crystal, R.G. 1989: Rapid, nonradioactive detection of mutations in the human genome by allele-specific amplification Journal of Laboratory and Clinical Medicine 114(2): 105-113
Bell, L.; Sherwood, W.G. 1987: Current practices and improved recommendations for treating hereditary fructose intolerance Journal of the American Dietetic Association 87(6): 721-728
Bonini, J.A.; Hofmann, C. 1991: A rapid, accurate, nonradioactive method for quantitating RNA on agarose gels Biotechniques 11(6): 708-710
Lebedeva, I.V.; Ivanovskaia, M.G.; Fedorov, A.N.; Limborskaia, S.A.; Shabarova, Z.A. 1994: A new method of nonradioactive labelling of oligonucleotides and their use as allele-specific probes for detecting mutations causing beta-thalassemia Molekuliarnaia Biologiia 28(4): 796-804
Lustig, A. 2004: Simple method to detect factors influencing drug expenditures Harefuah 143(1): 28-32; 85
Watkins, J.B.; Schoeller, D.A.; Klein, P.D.; Ott, D.G.; Newcomer, A.D.; Hofmann, A.F. 1977: 13C-trioctanoin: a nonradioactive breath test to detect fat malabsorption Journal of Laboratory and Clinical Medicine 90(3): 422-430
Baker, J.S.; Ederer, G.M.; Mundschenk, D. 1983: Particle size distribution analysis as a rapid method to detect significant bacteriuria American Journal of Medical Technology 49(10): 727-732